RN7SL493P
pseudogene in the species Homo sapiens
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RN7SL493P
Summary
RN7SL493P is a pseudogene[1].
Key Facts
- RN7SL493P's instance of is recorded as pseudogene[2].
- RN7SL493P's instance of is recorded as gene[3].
- RN7SL493P is a type of pseudogene[4].
- RN7SL493P's genomic start is recorded as 10221775[5].
- RN7SL493P's genomic end is recorded as 10222073[6].
- RN7SL493P's found in taxon is recorded as Homo sapiens[7].
- RN7SL493P's chromosome is recorded as human chromosome 16[8].
- RN7SL493P's strand orientation is recorded as reverse strand[9].
- RN7SL493P's exact match is recorded as http://identifiers.org/ncbigene/106479403[10].
- RN7SL493P's cytogenetic location is recorded as 16p13.2[11].
- RN7SL493P's expressed in is recorded as human kidney[12].
- RN7SL493P's expressed in is recorded as testicle[13].
- RN7SL493P's expressed in is recorded as gonad[14].
- RN7SL493P's expressed in is recorded as tonsil[15].
- RN7SL493P's expressed in is recorded as skeletal muscle tissue[16].
- RN7SL493P's expressed in is recorded as lymph node[17].
- RN7SL493P's expressed in is recorded as monocyte[18].
- RN7SL493P's expressed in is recorded as bone marrow[19].
- RN7SL493P's expressed in is recorded as prefrontal cortex[20].
- RN7SL493P's expressed in is recorded as stomach[21].